Quality Control Manager

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process. Quality Control Manager Full Time Mid-Level Managers Concord, OH, US 6 days ago Requisition ID: 1127 Job Responsibilities: Support QC functions related to GXP activities (e.g., cGMP manufacture of clinical and commercial active pharmaceutical ingredients) Manage laboratories that perform finished product testing of clinical and commercial materials Streamline current processes and procedures to provide consistent, timely performance Review and approve certificates of analysis received from contract laboratories Review and approve deviations related to QC activities Review OOS and OOT Investigations Support audits of contract laboratories in cooperation with Quality Assurance Review raw materials, in process and finished product specifications (purchasing, release and stability) Perform trend analysis of testing data to establish purchasing and release specifications for in process and finished product Assist with preparation and review of regulatory filings Assist with preparation, review and approval of APRs Create, edit, review and approve SOPs Qualifications: Minimum of 7 years of experience in the pharmaceutical industry and quality systems Minimum of 3 years of QC laboratory experience Bachelor's Degree in life sciences, preferably chemistry Experience in regulated manufacturing environments including regulatory authority inspections Strong written and verbal communication skills Demonstrated experience in structured process improvement Experience performing oversight and audits of laboratories Experience reviewing and approving raw data, test results and certificates of analysis for raw materials, drug product intermediates and final product Experience reviewing and approving method transfer and method validation protocols and reports #J-18808-Ljbffr